rel-(3S,4S)-3-Fluoro-4-methoxypyrrolidine hydrochloride

98%

Reagent Code: #233274
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CAS Number 2108511-81-3

science Other reagents with same CAS 2108511-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.6 g/mol
Formula C₅H₁₁ClFNO
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MDL Number MFCD23105900
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring high stereochemical precision. Its 3-fluoro-4-methoxypyrrolidine structure enhances metabolic stability, lipophilicity for improved cell permeability, and binding affinity in drug candidates, making it valuable in medicinal chemistry for CNS agents, antiviral drugs, and enzyme inhibitors. The hydrochloride salt form improves solubility and handling in synthetic processes.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿23,750.00
rel-(3S,4S)-3-Fluoro-4-methoxypyrrolidine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring high stereochemical precision. Its 3-fluoro-4-methoxypyrrolidine structure enhances metabolic stability, lipophilicity for improved cell permeability, and binding affinity in drug candidates, making it valuable in medicinal chemistry for CNS agents, antiviral drugs, and enzyme inhibitors. The hydrochloride salt form improves solubility and handling in synthetic processes.<

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring high stereochemical precision. Its 3-fluoro-4-methoxypyrrolidine structure enhances metabolic stability, lipophilicity for improved cell permeability, and binding affinity in drug candidates, making it valuable in medicinal chemistry for CNS agents, antiviral drugs, and enzyme inhibitors. The hydrochloride salt form improves solubility and handling in synthetic processes.

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